Canonical Allele Identifier: CA565934326
Gene: TDP2 HGNC NCBI

Linked Data

dbSNP Id: rs1357345623
gnomAD v2: 6-24658592-C-T
gnomAD v3: 6-24658364-C-T
gnomAD v4: 6-24658364-C-T
MyVariant Identifiers: chr6:g.24658592C>T (hg19) chr6:g.24658364C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24658364C>T , CM000668.2:g.24658364C>T GRCh38
NC_000006.11:g.24658592C>T , CM000668.1:g.24658592C>T GRCh37
NC_000006.10:g.24766571C>T NCBI36
NG_052787.1:g.13524G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378198.9:c.425+197G>A MANE Select ENSP00000367440.4:n.425+197G>A
ENST00000341060.3:c.251+197G>A ENSP00000345345.3:n.251+197G>A
ENST00000378198.8:c.425+197G>A ENSP00000367440.4:n.425+197G>A
ENST00000478285.1:n.612+197G>A
ENST00000478507.1:n.320-5211G>A
NM_016614.2:c.425+197G>A NP_057698.2:n.425+197G>A
XR_926244.1:n.552+197G>A
NM_016614.3:c.425+197G>A MANE Select NP_057698.2:n.425+197G>A
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